December 4, 2017 — Change Healthcare and Zebra Medical Vision announced an agreement to create solutions that deliver ...
The importance of quantitative analysis in breast imaging was the focus of numerous abstracts accepted for presentation at the 103rd Annual Radiological Society of North America (RSNA) meeting, Nov. 26-Dec. 1 in Chicago. Four abstracts highlighted the use of Volpara Solutions' quantitative analysis tools for breast imaging. The tools provide actionable quantitative metrics for clinicians, including volumetric density, personalized dose, potential high risk, and other factors designed to maintain accuracy and drive consistent quality in breast screening.
ScImage Inc. introduced PicomPassport at the Radiological Society of North America’s 103rd Annual Scientific Assembly, Nov. 26-Dec. 1 in Chicago. PicomPassport is a new technology that leverages PICOM365’s Azure-based Cloud to simplify the importing of external patient exams into any picture archiving and communication system (PACS).
eHealth Saskatchewan plays a vital role in providing IT services to patients, health care providers, and partners such ...
November 29, 2017 — Philips announced the introduction of IntelliSpace Enterprise Edition for Radiology, its ...
November 28, 2017 — Hologic Inc. announced it has signed a development and distribution agreement with Clarius Mobile ...

SPONSORED CONTENT — EnsightTM 2.0 is the newest version of Enlitic’s data standardization software framework. Ensight is ...
November 28, 2017 — Fujifilm Medical Systems U.S.A. Inc. displayed the all-new FDR Go Plus version portable digital ...
While most women understand the importance of health screenings, an estimated 72 million have missed or postponed a ...
Hologic Inc. announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Quantra 2.2 Breast Density Assessment Software. The software enables clinicians to provide women with consistent breast density assessments during routine breast cancer screenings.Hologic Inc. announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Quantra 2.2 Breast Density Assessment Software. The software enables clinicians to provide women with consistent breast density assessments during routine breast cancer screenings.Hologic Inc. announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Quantra 2.2 Breast Density Assessment Software. The software enables clinicians to provide women with consistent breast density assessments during routine breast cancer screenings. Hologic Inc. announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Quantra 2.2 Breast Density Assessment Software. The software enables clinicians to provide women with consistent breast density assessments during routine breast cancer screenings.
Infervision is introducing what it calls the first and only artificial intelligence (AI) platform to help radiologists detect and diagnose stroke faster, leading to patients getting life-saving treatment when time is of the essence. This new stroke detection solution is being introduced at the 2017 Radiological Society of North America (RSNA) conference, Nov. 26-Dec. 1 in Chicago.
November 27, 2017 — At the 103rd Scientific Assembly and Annual Meeting of the Radiological Society of North America ...
Fujifilm’s APERTO Lucent is a 0.4T mid-field, open MRI system addressing today’s capability and image quality needs ...
November 27, 2017 — Artificial intelligence (AI) startup Aidoc announced that it received CE (Conformité Européenne) ...
November 26, 2017 — Arterys Inc. announced the unveiling of their Arterys MICA platform at the 2017 Radiological Society ...
Samsung Electronics debuted its OmniTom mobile 16-slice computed tomography (CT) scanner at the Radiological Society of North America (RSNA) 2017 Annual Meeting, Nov. 26-Dec. 1 in Chicago. OmniTom received 510(k) U.S. Food and Drug Administration (FDA) clearance for the U.S. market on Aug. 18 of this year.
SPONSORED CONTENT — Fujifilm’s latest CT technology brings exceptional image quality to a compact and user- and patient ...
Lumedx Corp. will present the latest in cardiovascular (CV) imaging, data management and next-generation analytics solutions at the 103rd Scientific Assembly and Annual Meeting of the Radiological Society of North America (RSNA), Nov. 26-Dec. 1 in Chicago. The company said that they will showcase software developed to help heart and vascular hospitals improve outcomes, streamline the delivery of patient care and reduce costs.
November 22, 2017 — Intelerad Medical Systems announced that Diagnostic Centers of America (DCA) has selected Intelerad ...
Carestream Health announced its Carestream Touch Prime Ultrasound Systems have received a 2017 Innovative Technology designation from Vizient Inc., the largest member-driven healthcare performance improvement company in the country. The designation was based on direct feedback from hospital experts who interacted with the Touch Prime Ultrasound Systems at the Vizient Innovative Technology Exchange in Denver.
November 22, 2017 — Paxeramed will showcase its patient-centric imaging exchange, CareRad, at the 2017 Radiological ...
Augmented intelligence (also known as artificial intelligence, or AI) and machine learning are fueling innovations in healthcare to address the pressing clinical needs of care providers. At the 2017 Radiological Society of North America annual meeting (RSNA 2017), Nov. 26-Dec. 1 in Chicago, Agfa HealthCare will be demonstrating its latest work-in-progress visions for AI through workflow optimized integration of Agfa HealthCare's Enterprise Imaging solution with products offered by IBM Watson Health, RadLogics and Mindshare Medical.
Carestream Health will demonstrate new optional advanced metal artifact reduction software for its Carestream OnSight 3-D Extremity System at the 2017 Radiological Society of North America (RSNA) tradeshow, Nov. 26-Dec. 1 in Chicago. The system captures high-quality, low-dose 3-D extremity exams. The company’s new metal artifact reduction software is pending U.S. Food and Drug Administration (FDA) 510(k) clearance.
November 21, 2017 — At the 2017 Radiological Society of North America (RSNA) annual meeting, Nov. 26-Dec. 1 in Chicago ...
November 21, 2017 — Mevion Medical Systems announced the Mevion S250i Proton Therapy System has achieved CE Marking ...